Showing results (961-970 of 3,306) with videos related to
Sort By:
Pageof 331
Virus Genes|March 17, 2018
Proteomic analysis of A-549 cells infected with human adenovirus 40 by LC-MSAna Carla Peixoto Guissoni, Célia Maria Almeida Soares, Kareem R Badr, et al.British Journal of Pharmacology|April 27, 1999
Down-regulation of microglial cyclo-oxygenase-2 and inducible nitric oxide synthase expression by lipocortin 1L Minghetti, A Nicolini, E Polazzi, et al.Archives of Gynecology and Obstetrics|May 7, 2011
The history of vaginal birthRaphael Câmara Medeiros Parente, Lílian Paglarelli Bergqvist, Marina Bento Soares, et al.Journal of Cellular Physiology|June 26, 2010
Role of Annexin A1 in mouse myoblast cell differentiationValentina Bizzarro, Bianca Fontanella, Silvia Franceschelli, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 15, 2010
Cognitive estimation abilities in healthy and clinical populations: the use of the Cognitive Estimation TestGabriela Peretti Wagner, Sarah E MacPherson, Maria Alice M P Parente, et al.Biochemical Pharmacology|August 18, 2016
Matrix metalloproteinase (MMP)-2 decreases calponin-1 levels and contributes to arterial remodeling in early hypertensionVanessa de Almeida Belo, Juliana Montenegro Parente, José Eduardo Tanus-Santos, et al.La Ricerca in Clinica E in Laboratorio|July 1, 1981
Lymphocyte hyporesponsiveness during edema, proteinuria and hypertension (EPH) gestosisL Cagnoli, S Pasquali, M Mandreoli, et al.Journal of Neuroimmunology|September 1, 1995
Evidence that the interleukin-1 beta-induced prostaglandin E2 release from rat hypothalamus is mediated by type I and type II interleukin-1 receptorsA Mirtella, G Tringali, G Guerriero, et al.American Journal of Veterinary Research|July 1, 1993
Keratan sulfate as a marker of articular cartilage catabolism and joint treatment in poniesR J Todhunter, A E Yeager, K P Freeman, et al.Pediatric Neurology|March 18, 2014
Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?Antonino Romeo, Monica Lodi, Maurizio Viri, et al.Pageof 331